Cancer Res Treat. 2002 Jun;34(3):234-8. doi: 10.4143/crt.2002.34.3.234.
This study was performed to detect malignant cells in suspicious cases of malignant pleural effusion by cytogenetic analysis. MATERIALS AND METGODS: Eleven cases with pleural effusion were included in this study. Cells in pleural effusion were treated by direct, or short term, culture to prepare chromosomes. To analyze chromosomes, the G-banding method was used.
Chromosome preparations succeeded in 10 cases. 5 cases had normal karyotypes, but in 2 of these cases malignant cells were detected on cytological examination. The other 5 cases had abnormal chromosomes, but on cytological examination showed normal cell appearances.
Cytogenetic analysis of pleural effusions is not used routinely, but is more sensitive than the cytological examination of malignant pleural effusions. So, chromosome analysis is a good diagnostic tool, when chromosomal abnormalities are detected in an effusion. If a combination of cytology and cytogenetic study are used, the chance of detecting malignant cells in pleural effusion will be higher, and then more invasive diagnostic procedures, such as thoracoscopy or thoracotomy, could be avoided.
本研究通过细胞遗传学分析,旨在检测可疑恶性胸腔积液中的恶性细胞。
本研究纳入了 11 例胸腔积液患者。通过直接或短期培养处理胸腔积液中的细胞,以制备染色体。采用 G 带法分析染色体。
10 例患者的染色体制备成功。5 例患者具有正常核型,但其中 2 例在细胞学检查中发现恶性细胞。另外 5 例患者具有异常染色体,但细胞学检查显示正常细胞形态。
胸腔积液的细胞遗传学分析不常规进行,但比恶性胸腔积液的细胞学检查更敏感。因此,当在胸腔积液中检测到染色体异常时,染色体分析是一种很好的诊断工具。如果将细胞学和细胞遗传学研究相结合,可以提高胸腔积液中恶性细胞的检出率,从而避免进行更具侵袭性的诊断程序,如胸腔镜或开胸手术。